gb Ideal PCR Master Mix
gb Ideal PCR Master Mix is intended for research PCR and real-time PCR applications with fluorescently labelled probes and with high sensitivity and efficiency request. It is not intended for use in diagnostics.
Description of the product
gb Ideal PCR Master Mix consists of hot-start Taq DNA polymerase, reaction buffer, dNTP and MgCl2. Taq polymerase is chemically modified DNA polymerase from Thermus aquaticus. This polymerase is completely inactive at room temperature but it is rapidly activated during the initial denaturation step of PCR.
Parameters of the product
- Master Mix is a 2× concentrated solution.
- It contains all the components necessary for PCR performance.
- It is specified especially for real-time PCR applications demanding high sensitivity, for example microbial DNA detection and somatic mutations detection. Master Mix is enriched with components which preventPCR reaction inhibition through which higher reliability of the detection is ensured.
- Polymerase is a hot-start type with a short activation time (3 min / 95 °C), with 5´-3´ polymerase and exonuclease activity, 3´-5´ exonuclease activity is not present.
gb PCR Master Mix by application
|
gb Ideal |
end-point PCR, common PCR amplification |
|
real-time PCR without probes |
|
real-time PCR with hydrolysis probes |
✓
|
real-time PCR with LNA probes |
✓
|
real-time PCR with hybridization probes |
|
real-time PCR with High Resolution Melting Analysis |
|
real-time PCR with low DNA samples |
✓
|
real-time PCR with inhibited samples |
|